This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wireman, J.
Right arrow Articles by Summers, A. O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wireman, J.
Right arrow Articles by Summers, A. O.
Agricola
Right arrow Articles by Wireman, J.
Right arrow Articles by Summers, A. O.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol., Nov 1997, 4494-4503, Vol 63, No. 11
Copyright © 1997, American Society for Microbiology

Association of mercury resistance with antibiotic resistance in the gram-negative fecal bacteria of primates

J Wireman, CA Liebert, T Smith and AO Summers
Department of Microbiology, University of Georgia, Athens 30602-2605, USA.

Gram-negative fecal bacterial from three longitudinal Hg exposure experiments and from two independent survey collections were examined for their carriage of the mercury resistance (mer) locus. The occurrence of antibiotic resistance was also assessed in both mercury- resistant (Hgr) and mercury-susceptible (Hgs) isolates from the same collections. The longitudinal studies involved exposure of the intestinal flora to Hg released from amalgam "silver" dental restorations in six monkeys. Hgr strains were recovered before the installation of amalgams, and frequently these became the dominant strains while amalgams were installed. Such persistent Hgr strains always carried the same mer locus throughout the experiments. In both the longitudinal and survey collections, certain mer loci were preferentially associated with one genus, whereas other mer loci were recovered from many genera. In general, strains with any mer locus were more likely to be multiresistant than were strains without mer loci; this clustering tendency was also seen for antibiotic resistance genes. However, the association of antibiotic multiresistance with mer loci was not random; regardless of source, certain mer loci occurred in highly multiresistant strains (with as many as seven antibiotic resistances), whereas other mer loci were found in strains without any antibiotic resistance. The majority of highly multiresistant Hgr strains also carried genes characteristic of an integron, a novel genetic element which enables the formation of tandem arrays of antibiotic resistance genes. Hgr strains lacking antibiotic resistance showed no evidence of integron components.


This article has been cited by other articles:

  • Roberts, M.C., Leroux, B.G., Sampson, J., Luis, H.S., Bernardo, M., Leitao, J. (2008). Dental Amalgam and Antibiotic- and/or Mercury-resistant Bacteria. JDR 87: 475-479 [Abstract] [Full Text]  
  • Williams, L. E., Detter, C., Barry, K., Lapidus, A., Summers, A. O. (2006). Facile recovery of individual high-molecular-weight, low-copy-number natural plasmids for genomic sequencing.. Appl. Environ. Microbiol. 72: 4899-4906 [Abstract] [Full Text]  
  • Nandi, S., Maurer, J. J., Hofacre, C., Summers, A. O. (2004). Gram-positive bacteria are a major reservoir of Class 1 antibiotic resistance integrons in poultry litter. Proc. Natl. Acad. Sci. USA 101: 7118-7122 [Abstract] [Full Text]  
  • Schelert, J., Dixit, V., Hoang, V., Simbahan, J., Drozda, M., Blum, P. (2004). Occurrence and Characterization of Mercury Resistance in the Hyperthermophilic Archaeon Sulfolobus solfataricus by Use of Gene Disruption. J. Bacteriol. 186: 427-437 [Abstract] [Full Text]  
  • Essa, A. M. M., Julian, D. J., Kidd, S. P., Brown, N. L., Hobman, J. L. (2003). Mercury Resistance Determinants Related to Tn21, Tn1696, and Tn5053 in Enterobacteria from the Preantibiotic Era. Antimicrob. Agents Chemother. 47: 1115-1119 [Abstract] [Full Text]  
  • Pike, R., Lucas, V., Stapleton, P., Gilthorpe, M. S., Roberts, G., Rowbury, R., Richards, H., Mullany, P., Wilson, M. (2002). Prevalence and antibiotic resistance profile of mercury-resistant oral bacteria from children with and without mercury amalgam fillings. J Antimicrob Chemother 49: 777-783 [Abstract] [Full Text]  
  • McArthur, J V., Tuckfield, R. C. (2000). Spatial Patterns in Antibiotic Resistance among Stream Bacteria: Effects of Industrial Pollution. Appl. Environ. Microbiol. 66: 3722-3726 [Abstract] [Full Text]  
  • Mazel, D., Dychinco, B., Webb, V. A., Davies, J. (2000). Antibiotic Resistance in the ECOR Collection: Integrons and Identification of a Novel aad Gene. Antimicrob. Agents Chemother. 44: 1568-1574 [Abstract] [Full Text]  
  • Leistevuo, J., Järvinen, H., Österblad, M., Leistevuo, T., Huovinen, P., Tenovuo, J. (2000). Resistance to Mercury and Antimicrobial Agents in Streptococcus mutans Isolates from Human Subjects in Relation to Exposure to Dental Amalgam Fillings. Antimicrob. Agents Chemother. 44: 456-457 [Abstract] [Full Text]  
  • Bass, L., Liebert, C. A., Lee, M. D., Summers, A. O., White, D. G., Thayer, S. G., Maurer, J. J. (1999). Incidence and Characterization of Integrons, Genetic Elements Mediating Multiple-Drug Resistance, in Avian Escherichia coli. Antimicrob. Agents Chemother. 43: 2925-2929 [Abstract] [Full Text]  
  • Liebert, C. A., Hall, R. M., Summers, A. O. (1999). Transposon Tn21, Flagship of the Floating Genome. Microbiol. Mol. Biol. Rev. 63: 507-522 [Abstract] [Full Text]